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Updated: Mar 26, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
[Current status of castration-resistant prostate cancer translational research]
Abstract:
Recently, new drugs including abiraterone and enzalutamide have been able to be used for castration resistant prostate cancer(CRPC) patients. However, a subset of these patients who receive the new drugs does not response to the therapies. Furthermore, most patients who initially response to the drugs, progress to secondary resistance eventually. Therefore, it is important to investigate a novel therapeutic target and a novel treatment-selection marker for CRPC. In this review, we focused on AR-V7, TMPRSS2-ERG fusion gene and EP4 antagonist as representative translational researches.
Insights
New treatments for castration-resistant prostate cancer (CRPC) show limited efficacy. This review explores novel therapeutic targets like AR-V7, TMPRSS2-ERG, and EP4 antagonists to overcome treatment resistance in CRPC patients.
Area of Science:
- Oncology
- Translational Research
Background:
- Castration-resistant prostate cancer (CRPC) poses a significant clinical challenge.
- While abiraterone and enzalutamide offer new treatment options, a subset of patients exhibit primary resistance, and most eventually develop secondary resistance.
Purpose of the Study:
- To review novel therapeutic targets and treatment-selection markers for CRPC.
- To highlight translational research on AR-V7, TMPRSS2-ERG fusion gene, and EP4 antagonists.
Main Methods:
- Literature review focusing on recent advancements in CRPC therapy.
- Analysis of translational research on specific molecular targets.
Main Results:
- Identified AR-V7, TMPRSS2-ERG fusion gene, and EP4 antagonists as promising areas for CRPC research.
- These targets represent potential strategies to overcome therapeutic resistance.
Conclusions:
- Further investigation into AR-V7, TMPRSS2-ERG, and EP4 antagonists is crucial for developing more effective CRPC treatments.
- These targets may serve as biomarkers for selecting appropriate therapies and overcoming resistance mechanisms.
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